Indinavir/ritonavir remains an important component of HAART for the treatment of HIV/AIDS, particularly in resource-limited settings

被引:12
作者
Cressey, Tim R.
Plipat, Nottasorn
Fregonese, Federica
Chokephaibulkit, Kulkanya
机构
[1] Chiang Mai Univ, Program HIV Prevent & Treatment PHPT IRD174, Chiang Mai 50205, Thailand
[2] Harvard Univ, Sch Publ Hlth, Boston, MA 02115 USA
[3] Univ Michigan, Sch Publ Hlth, Dept Epidemiol, Ann Arbor, MI 48109 USA
[4] Mahidol Univ, Siriraj Hosp, Fac Med, Dept Pediat, Bangkok 10700, Thailand
关键词
antiretrovirals; HIV; indinavir; ritonavir; Thailand; tolerance;
D O I
10.1517/17425255.3.3.347
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
For over a decade, indinavir has been approved for the treatment of HIV/AIDS; however, following the introduction of new protease inhibitors (Pls) with improved safety and pharmacologic profiles, its use in developed countries has become almost obsolete. In contrast, in resource-limited settings where the majority of people living with HIV/AIDS reside, indinavir is part of the most affordable PI-based highly active antiretroviral treatment regimen. A major drawback of indinavir use is renal toxicity, but low-dose indinavir plus ritonavir (400/100 mg) twice daily is both efficacious and tolerable. Similar low dosing levels in children have also proven successful, but data in pregnant women remains limited. Due to its low cost and proven efficacy indinavir remains a key component of HIV/AIDS treatment in resource-limited settings.
引用
收藏
页码:347 / 361
页数:15
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